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Autoradiographic analysis of GABA‐benzodiazepine receptors in an animal model of acute hepatic encephalopathy
Author(s) -
Rössle Martin,
Deckert Jürgen,
Jones E. Anthony
Publication year - 1989
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.1840100204
Subject(s) - hepatic encephalopathy , flunitrazepam , gabaa receptor , benzodiazepine , fulminant hepatic failure , medicine , muscimol , aminobutyric acid , endocrinology , receptor , flumazenil , cerebellum , chemistry , cerebral cortex , hippocampus , pharmacology , biology , cirrhosis , transplantation , liver transplantation
To complement analogous studies using conventional ligand‐membrane binding assays, the densities of γ‐aminobutyric acid and benzodiazepine receptors in the brain have been assessed using an autoradiographic technique in an animal model of hepatic encephalopathy. Hepatic encephalopathy due to fulminant hepatic failure was induced in rabbits by the intravenous injection of galactosamine. The specific binding of three radiolabeled ligands was assessed densitometrically in several microregions of cerebral cortex, hippocampus and cerebellum. [ 3 H]Muscimol was used to assess γ‐aminobutyric acid receptor density and [ 3 H]flunitrazepam or [ 3 H]Ro 15–1788 was used to assess benzodiazepine receptor density. No significant differences were observed between the magnitude of binding of the three ligands to each of the microregions of brain from control rabbits and rabbits in Stage III or IV hepatic encephalopathy. These findings suggest that the behavioral expression of hepatic encephalopathy in the model studied is not dependent upon an increase in the number of γ‐aminobutyric acid or benzodiazepine receptors, but do not conflict with the hypothesis that γ‐aminobutyric acid‐ergic tone is increased in hepatic encephalopathy.